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  4. A Subpopulation of Foxj1-Expressing, Nonmyelinating Schwann Cells of the Peripheral Nervous System Contribute toSchwannCellRemyelinationintheCentralNervousSystem

A Subpopulation of Foxj1-Expressing, Nonmyelinating Schwann Cells of the Peripheral Nervous System Contribute toSchwannCellRemyelinationintheCentralNervousSystem

The Journal of Neuroscience, 2018 · DOI: 10.1523/JNEUROSCI.0585-18.2018 · Published: October 24, 2018

Regenerative MedicineNeurologyGenetics

Simple Explanation

Remyelination failure in chronic demyelinating diseases such as multiple sclerosis drives the current quest for developing means by which remyelination in CNS can be enhanced therapeutically. Critical to this endeavor is the need to understand the mechanisms of remyelination, including the nature and identity of the cells capable of generating new myelin sheath-forming cells. Here, we report a previously unrecognized subpopulation of nonmyelinating Schwann cells (SCs) in the PNS, identified by the expression of the transcription factor Foxj1, which can give rise to SCs that are capable of remyelinating both PNS and CNS axons.

Study Duration
Not specified
Participants
Mice with C57BL6 background expressing Foxj1-CreERT2
Evidence Level
Not specified

Key Findings

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    A subpopulation of nonmyelinating Schwann cells identified by Foxj1 expression contributes to CNS SC remyelination, as well as remyelination in the PNS.
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    Ependymal cells lining the central canal of the spinal cord, which also express Foxj1, do not generate cells that contribute to CNS remyelination.
  • 3
    Foxj1-expressing cells in peripheral nerves respond to peripheral nerve injury and give rise to repair SCs

Research Summary

This study identifies a previously unrecognized population of PNS glia that can participate in the regeneration of new myelin sheaths following CNS demyelination. The findings show that Foxj1 is also expressed by a population of NMSCs and that these cells can give rise to remyelinating SCs in the CNS. Following demyelination of the ventral spinal cord, many remyelinating SCs came from Foxj1-labeled cells from peripheral nerves.

Practical Implications

Therapeutic Target

Foxj1-expressing nonmyelinating Schwann cells represent a new cellular target for myelin regenerative strategies.

Understanding Remyelination

Further research into the mechanisms by which Foxj1+ NMSCs contribute to remyelination can lead to more effective therapies.

Clinical Relevance

These cells therefore represent a new cellular target for myelin regenerative strategies for the treatment of CNS disorders characterized by persistent demyelination.

Study Limitations

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